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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133193Generated: October 30, 2026

Water → HCID 59735302, compound

https://huagongshe.com/reaction/133193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-OxazolidinoneHCID 73949—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59735302HCID 5973530266%

Reaction Steps

To a solution containing the oxazolidinone (5.0 g, 13.9 mmol) in dry THF (50 mL) was added potassium-t-butoxide (2.03 g, 18.1 mmol, 1.3 equiv) at RT and stirred under N2 atm for 0.5 h. To this solution was added ethyl iodide (3.25 g, 20.8 mmol, 1.5 equiv) and stirred for 2 h after which TLC (1:1 hex-EtOAc) showed completion of reaction. The reaction was quenched by adding satd. NH4Cl solution. THF was removed on rotovap and residue diluted with CH2Cl2 (100 mL). Organic layer washed with brine and dried (MgSO4). Removal of solvent gave a light yellow oil. This crude product was taken in CH2Cl2 (50 mL). Added trifluoroacetic acid (4.75 g, 41.7 mmol, 3.0 equiv)-water (1.0 g, 55.5 mmol, 4 equiv) dropwise and stirred for 2 h. The solvent was removed on rotovap and residue purified by flash column chromatography (silica gel, EtOAc) to get the product as a colorless oil (1.3 g, 66% in two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390825B1
Source datasetuspto-grants-2008_06
ORD IDord-f91bab0e5ce442f8be062c492383b636
Source noteuspto-grants-2008_06